ClinVar Miner

List of variants reported as pathogenic for Immunodeficiency 27A

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Total variants: 14
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HGVS dbSNP gnomAD frequency
NM_000416.3(IFNGR1):c.260T>C (p.Ile87Thr) rs104893973 0.00002
NM_000416.3(IFNGR1):c.2T>A (p.Met1Lys) rs387906593 0.00002
NM_000416.3(IFNGR1):c.523del (p.Tyr175fs) rs749956849 0.00001
NC_000006.11:g.(?_136482728)_(137540520_?)del
NM_000416.3(IFNGR1):c.104_107dup (p.Ile37fs) rs587776854
NM_000416.3(IFNGR1):c.131del (p.Pro44fs) rs587776853
NM_000416.3(IFNGR1):c.182T>A (p.Val61Glu) rs121912715
NM_000416.3(IFNGR1):c.200+1G>A rs587776855
NM_000416.3(IFNGR1):c.230G>A (p.Cys77Tyr) rs104893974
NM_000416.3(IFNGR1):c.295_306del (p.Trp99_Val102del) rs587776857
NM_000416.3(IFNGR1):c.446C>A (p.Ser149Ter) rs387906572
NM_000416.3(IFNGR1):c.476del (p.Val159fs) rs1582635229
NM_000416.3(IFNGR1):c.653_655del (p.Glu218del) rs587776858
NM_000416.3(IFNGR1):c.86-1_93del rs753213766

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